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221013 ||| eng |
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|a Ganslandt, Mattias
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|a Parallel imports of pharmaceutical products in the European Union
|h Elektronische Ressource
|c Mattias Ganslandt and Keith E. Maskus
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| 260 |
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|a Washington, D.C
|b World Bank, Development Research Group, Trade
|c 2001
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| 653 |
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|a Drugs / Prices / European Union countries / Econometric models
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| 653 |
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|a Price regulation / European Union countries / Econometric models
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| 653 |
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|a Gray market / European Union countries / Econometric models
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| 653 |
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|a Imports / European Union countries / Econometric models
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| 653 |
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|a Trademarks (International law) / Econometric models
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| 700 |
1 |
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|a Maskus, Keith Eugene
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| 710 |
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|a World Bank
|b Development Research Group
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|a eng
|2 ISO 639-2
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| 989 |
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|b WOBA
|a World Bank E-Library Archive
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|a Policy research working paper
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|a "July 2001. - Includes bibliographical references (p. 22). - Title from title screen as viewed on Sept. 07, 2002
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|u http://elibrary.worldbank.org/content/workingpaper/10.1596/1813-9450-2630
|x Verlag
|3 Volltext
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|a 330
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|a Parallel imports are legitimately produced goods imported legally into a country without the authorization of a trademark, copyright, or patent holder. In the European Union, so long as a pharmaceutical manufacturer has placed a good on the market voluntarily, the principle of free movement of goods allows individuals or firms within the EU to trade goods across borders without the consent of the producer. What is the effect of these parallel imports?
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